COmparison of PENG Block and SIFICB in Hip Fracture Surgeries

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age40-80
SponsorAdiyaman University Research Hospital

About this trial

The aim of this study is to compare the effectiveness of the PENG block and SIFIB in facilitating the positioning for neuroaxial anesthesia and their impact on the quality of postoperative analgesia.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Hip fractures

40-80 years

Disqualifiers

Contraindicated to spinal anesthesia

allergy to local anesthetics

severe peripheral neuropathy

mental disorders

Trial design

Design model

Parallel

Treatments tested in this trial

  • PENG Block

    Procedure/Surgery

    The PENG block will be performed on the patient with the injection of local anesthesia under ultrasound guidance in the femoral region, beneath the biceps tendon.

  • SIFICB Block

    Procedure/Surgery

    The SIFIB block will be performed on the patient with the injection of local anesthetic between the iliac fascia and iliac muscle in the femoral region, under ultrasound guidance.

Treatment groups

150 Participants
are divided into 2 treatment groups
Group A: Group PExperimental treatment 1 intervention
Group B: Group SExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Patient positioning

In patients with hip fractures, during spinal anesthesia, the angle between the patient's back and the operating table will be recorded while positioning the patient.

Time frame
During neuroaxial block procedure

Secondary outcomes

1

Visual Analog Scale (VAS) score

VAS score is a measurement instrument for subjective characteristics of pain. VAS score range from 0 to 10. 0 refers to no pain and 10 refers to the worst pain ever had

Time frame
During neuroaxial block procedure

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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